Reconfigurable Acceleration of Short Read Mapping

Recent improvements in the throughput of next-generation DNA sequencing machines poses a great computational challenge in analysing the massive quantities of data produced. This paper proposes a novel approach, based on reconfigurable computing technology, for accelerating short read mapping, where the positions of millions of short reads are located relative to a known reference sequence. Our approach consists of two key components: an exact string matcher for the bulk of the alignment process, and an approximate string matcher for the remaining cases. We characterise interesting regions of the design space, including homogeneous, heterogeneous and run-time reconfigurable designs and provide back of envelope estimations of the corresponding performance. We show that a particular implementation of this architecture targeting a single FPGA can be up to 293 times faster than BWA on an Intel X5650 CPU, and 134 times faster than SOAP3 on an NVIDIA GTX 580 GPU.